Assistant Director for Plasma Operations

5 days ago


Provo, Utah, United States Grifols Canada Therapeutics Inc Full time
Job Summary

We are seeking an experienced and skilled Assistant Manager for Plasma Center to join our team at Grifols Canada Therapeutics Inc. The successful candidate will be responsible for overseeing all aspects of the donor center when the Center Manager is not present.

Key Responsibilities
  • Creates an organizational environment that stimulates morale and productivity of the workforce and its leadership.
  • Collaborates with Training and Quality staff to ensure training and quality goals are met.
  • Coaches and leads employees through effective feedback.
  • Monitors and evaluates operations, developing action plans to maximize center efficiency.
  • Responsible for all personnel functions, including hiring, assignment, and direction of work.
  • Directs the training activities of production employees.
  • Partners with the center manager in budget preparation and oversees facility to achieve production targets and quality goals.
  • Reviews and approves employee schedules to accommodate donor cycles.
  • Actively delegates, monitors, and holds responsible operations supervisors for their performance.
  • Determines the adequacy and adjusts inventory levels of all goods and supplies necessary for the operation of the donor center.
  • Assures center employees maintain the facility in a neat and clean condition and all equipment is kept in good working order.
  • Responsible for freezer management, including overseeing plasma shipments and equipment failures.
  • Constructs and submits timely and accurate reports on a daily/weekly/monthly or as required basis.
  • Develops and implements active donor recruitment advertising campaigns to improve production levels.
  • Maintains thorough familiarity and ensures compliance with state and federal regulations, U.S. Food and Drug Administration (FDA)-approved Standard Operating Procedures, Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), and Current Good Manufacturing Practice (cGMP).
Requirements
  • Bachelor's degree or equivalent in Science, Business, Nursing, Finance, or related field.
  • Typically requires 2 years of related experience in clinical or general business experience.
  • Supervisory experience preferred.
  • Experience in a medical and/or cGMP regulated environment preferred.
  • Experience with plasma or whole blood is a plus.
Attributes
  • Developing command of leadership, organizational, customer service, interpersonal communication, and computer abilities.
  • Ability to understand and assess FDA regulations.
  • Ability to maintain adequate levels of plasma collection and adhere to quality standards.
  • Ability to motivate staff to achieve established goals and standards.

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